(E)-4-(propen-1-yl)-5,6-dihydro-2H-pyran-2-one

Details

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Internal ID 94ce00fa-0d29-429a-9a8b-3c286e9f3f0d
Taxonomy Organoheterocyclic compounds > Pyrans > Pyranones and derivatives > Dihydropyranones
IUPAC Name 4-[(E)-prop-1-enyl]-2,3-dihydropyran-6-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C8H10O2/c1-2-3-7-4-5-10-8(9)6-7/h2-3,6H,4-5H2,1H3/b3-2+
InChI Key KUOMSAOBPORCBU-NSCUHMNNSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C8H10O2
Molecular Weight 138.16 g/mol
Exact Mass 138.068079557 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 1.20
Atomic LogP (AlogP) 1.44
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (E)-4-(propen-1-yl)-5,6-dihydro-2H-pyran-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9934 99.34%
Caco-2 + 0.9097 90.97%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Mitochondria 0.6881 68.81%
OATP2B1 inhibitior - 0.8648 86.48%
OATP1B1 inhibitior + 0.9251 92.51%
OATP1B3 inhibitior + 0.9607 96.07%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.9097 90.97%
P-glycoprotein inhibitior - 0.9940 99.40%
P-glycoprotein substrate - 0.9531 95.31%
CYP3A4 substrate - 0.6544 65.44%
CYP2C9 substrate - 0.6171 61.71%
CYP2D6 substrate - 0.9003 90.03%
CYP3A4 inhibition - 0.9531 95.31%
CYP2C9 inhibition - 0.9282 92.82%
CYP2C19 inhibition - 0.7958 79.58%
CYP2D6 inhibition - 0.9314 93.14%
CYP1A2 inhibition - 0.6840 68.40%
CYP2C8 inhibition - 0.9770 97.70%
CYP inhibitory promiscuity - 0.9003 90.03%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8628 86.28%
Carcinogenicity (trinary) Non-required 0.5475 54.75%
Eye corrosion + 0.6138 61.38%
Eye irritation + 0.9935 99.35%
Skin irritation + 0.6390 63.90%
Skin corrosion - 0.9257 92.57%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6703 67.03%
Micronuclear - 0.8700 87.00%
Hepatotoxicity + 0.6824 68.24%
skin sensitisation - 0.5888 58.88%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity - 0.7111 71.11%
Mitochondrial toxicity - 0.8125 81.25%
Nephrotoxicity + 0.6422 64.22%
Acute Oral Toxicity (c) III 0.6605 66.05%
Estrogen receptor binding - 0.9288 92.88%
Androgen receptor binding - 0.5108 51.08%
Thyroid receptor binding - 0.8931 89.31%
Glucocorticoid receptor binding - 0.7523 75.23%
Aromatase binding - 0.9365 93.65%
PPAR gamma - 0.8199 81.99%
Honey bee toxicity - 0.8937 89.37%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity + 0.5900 59.00%
Fish aquatic toxicity - 0.6684 66.84%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.02% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.27% 91.11%
CHEMBL2581 P07339 Cathepsin D 89.01% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.91% 86.33%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.50% 100.00%
CHEMBL230 P35354 Cyclooxygenase-2 81.77% 89.63%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.26% 94.45%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 146684245
LOTUS LTS0005450
wikiData Q105146269